NDC 54868-6183 Natazia
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
RED (C48326 - MEDIUM)
YELLOW (C48330 - LIGHT)
RED (C48326 - DARK)
WHITE (C48325)
DJ
DH
DN
DT
Code Structure Chart
Product Details
What is NDC 54868-6183?
What are the uses for Natazia?
Which are Natazia UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESTRADIOL VALERATE (UNII: OKG364O896)
- ESTRADIOL VALERATE (UNII: OKG364O896) (Active Moiety)
- DIENOGEST (UNII: 46M3EV8HHE)
- DIENOGEST (UNII: 46M3EV8HHE) (Active Moiety)
Which are Natazia Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE K25 (UNII: K0KQV10C35)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Natazia?
- RxCUI: 748797 - inert 1 MG Oral Tablet
- RxCUI: 748797 - inert ingredients 1 MG Oral Tablet
- RxCUI: 978941 - estradiol valerate 3 MG Oral Tablet
- RxCUI: 978944 - dienogest 2 MG / estradiol valerate 2 MG Oral Tablet
- RxCUI: 978946 - dienogest 3 MG / estradiol valerate 2 MG Oral Tablet
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".